No photo of Päivi T Peltomäki
  • PL 63 (Haartmaninkatu 8)

    00014

    Finland

1987 …2020

Research output per year

If you made any changes in Pure these will be visible here soon.

Personal profile

Fields of Science

  • 3111 Biomedicine

International and National Collaboration Publications and projects within past five years.

Publications

Thyroid carcinomas that occur in familial adenomatous polyposis patients recurrently harbor somatic variants in APC, BRAF, and KTM2D

Nieminen, T. T., Walker, C. J., Olkinuora, A., Genutis, L. K., O'Malley, M., Wakely Paul E, J., LaGuardia, L., Koskenvuo, L., Arola, J., Lepistö, A., Brock, P., Yilmaz, A. S., Eisfeld, A-K., Church, J., Peltomäki, P. & de la Chapelle, A., 1 Mar 2020, In : Thyroid. 30, 3, p. 380-388 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition

Swedish Extended Genetic Anal Colo, Olkinuora, A., Nieminen, T. T., Mårtensson, E., Rohlin, A., Ristimäki, A., Koskenvuo, L., Lepistö, A., Gebre-Medhin, S., Nordling, M. & Peltomäki, P., Aug 2019, In : Genetics In medicine. 21, 8, p. 1868-1873 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

DNA methylation changes and somatic mutations as tumorigenic events in Lynch syndrome-associated adenomas retaining mismatch repair protein expression

Mäki-Nevala, S., Valo, S., Ristimaki, A., Sarhadi, V., Knuutila, S., Nyström, M., Renkonen-Sinisalo, L., Lepistö, A., Mecklin, J-P. & Peltomäki, P., Jan 2019, In : EBioMedicine. 39, p. 280-291 12 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Epidemiological, clinical and molecular characterization of Lynch-like syndrome: A population-based study

Porkka, N., Lahtinen, L., Ahtiainen, M., Böhm, J. P., Kuopio, T., Eldfors, S., Mecklin, J-P., Seppälä, T. T. & Peltomäki, P., 1 Jul 2019, In : International Journal of Cancer. 145, 1, p. 87-98 12 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

How should we correctly interpret biallelic germline truncating variant of MLH3 in hereditary colorectal cancer? Response

Olkinuora, A., Nieminen, T. T., Nordling, M. & Peltomäki, P., Nov 2019, In : Genetics In medicine. 21, 11, p. 2652-2653 2 p.

Research output: Contribution to journalLetterScientific

Open Access
File

Projects

Prizes

Activities

Walter Pavicic

Päivi T Peltomäki (Host)
9 Jun 201824 Jun 2018

Activity: Hosting a visitor typesAcademic visit at UH

Walter Pavicic

Päivi T Peltomäki (Host)
15 Oct 20164 Dec 2016

Activity: Hosting a visitor typesAcademic visit at UH

Academic dissertation

Päivi T Peltomäki (Supervisor)
2015 → …

Activity: Examination typesSupervisor or co-supervisor of doctoral thesis

Academic dissertation

Päivi T Peltomäki (Supervisor)
2015 → …

Activity: Examination typesSupervisor or co-supervisor of doctoral thesis

Dr. Henry T. Lynch Symposium - Advances in Hereditary Cancer

Päivi T Peltomäki (Speaker: Presenter)
17 Sep 201518 Sep 2015

Activity: Participating in or organising an event typesPublic Talks

Press / Media

Radiaattori: Epigenetiikka

Päivi T Peltomäki

09/05/2007

1 Media contribution

Press/Media: Press / Media